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三丁基锡和 2,3,7,8-四氯二苯并对二恶英对分化的成骨细胞和破骨细胞的协同作用。

Synergistic effects of tributyltin and 2,3,7,8-tetrachlorodibenzo-p-dioxin on differentiating osteoblasts and osteoclasts.

机构信息

University of Oulu, Department of Anatomy and Cell Biology, Oulu, Finland.

出版信息

Toxicol Appl Pharmacol. 2012 Sep 1;263(2):210-7. doi: 10.1016/j.taap.2012.06.011. Epub 2012 Jun 27.

Abstract

The purpose of this study was to examine the effects of the persistent and accumulative environmental pollutants tributyltin (TBT) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) individually and in combination on differentiating bone cells. TBT and TCDD are chemically distinct compounds with different mechanisms of toxicity, but they typically have the same sources of exposure and both have been shown to affect bone development at low exposure levels. Bone marrow stem cells were isolated from femurs and tibias of C57BL/6J mice, differentiated in culture into osteoblasts or osteoclasts and exposed to 0.1-10nM TBT, 0.01-1nM TCDD or 10nM TBT+ 1nM TCDD. In osteoblasts, the combined exposure to TBT and TCDD significantly decreased the mRNA expression of alkaline phosphatase and osteocalcin more than TBT or TCDD alone. PCR array showed different gene expression profiles for TBT and TCDD individually, and the combination evoked several additional alterations in gene expression. Expression of aryl hydrocarbon receptor repressor (AHRR) was increased by TCDD as expected, but simultaneous exposure to TBT prevented the increase thus potentially strengthening AHR-mediated effects of TCDD. The number of osteoclasts was reduced by TCDD alone and in combination with TBT, but TBT alone had no effect. However, the total area of resorbed bone was remarkably lower after combined exposure than after TBT or TCDD alone. In conclusion, very low concentrations of TBT and TCDD have synergistic deleterious effects on bone formation and additive effects on bone resorption.

摘要

本研究旨在研究持久性和累积性环境污染物三丁基锡(TBT)和 2,3,7,8-四氯二苯并对二恶英(TCDD)单独及联合作用对分化骨细胞的影响。TBT 和 TCDD 是化学性质不同的化合物,其毒性机制也不同,但它们通常具有相同的暴露源,并且都已被证明在低暴露水平下会影响骨骼发育。从 C57BL/6J 小鼠的股骨和胫骨中分离出骨髓干细胞,在培养中分化为成骨细胞或破骨细胞,并暴露于 0.1-10nM TBT、0.01-1nM TCDD 或 10nM TBT+1nM TCDD。在成骨细胞中,TBT 和 TCDD 的联合暴露显著降低碱性磷酸酶和骨钙素的 mRNA 表达,比 TBT 或 TCDD 单独暴露更为明显。PCR 阵列显示 TBT 和 TCDD 单独作用时有不同的基因表达谱,联合作用还引起了几个额外的基因表达改变。AHRR 的表达如预期的那样被 TCDD 上调,但 TBT 的同时暴露阻止了这种增加,从而可能增强 TCDD 的 AHR 介导作用。TCDD 单独和与 TBT 联合作用均可减少破骨细胞数量,但 TBT 单独作用没有影响。然而,联合暴露后的骨吸收总面积明显低于 TBT 或 TCDD 单独暴露后的面积。总之,非常低浓度的 TBT 和 TCDD 对骨形成具有协同的有害影响,对骨吸收具有相加的作用。

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